Canonical Allele Identifier: CA2399817858

Gene: MN1

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.27750469G= , CM000684.2:g.27750469G=	GRCh38
NC_000022.10:g.28146457G= , CM000684.1:g.28146457G=	GRCh37
NC_000022.9:g.26476457G=	NCBI36
NG_023258.1:g.56030C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703102.1:n.934C=
ENST00000302326.5:c.*446C= MANE Select	ENSP00000304956.4:n.*446C=
ENST00000302326.4:c.*446C=	ENSP00000304956.4:n.*446C=
ENST00000424656.1:c.456-241C=
NM_002430.2:c.*446C=	NP_002421.3:n.*446C=
NM_002430.3:c.*446C= MANE Select	NP_002421.3:n.*446C=